Industry Architect, Life Sciences
SnowflakeFull Time
Expert & Leadership (9+ years)
Candidates should possess 3+ years of experience in one or more of the following industries and roles: commercial software (e.g., product management, solutions consulting, customer success), quality assurance, CMC, clinical development (e.g., clinical operations), pharmacovigilance, regulatory affairs, or regulatory operations in the life sciences industry. They must have working knowledge of regulatory processes and procedures in at least one regulated sector of the life sciences industry (e.g., regulatory, clinical, commercial, quality, pharmacovigilance).
The Regulatory Intelligence Analyst will identify regulatory requirements related to the product and implement best practices for monitoring, interpreting, and communicating changes to internal teams, proactively monitor the global regulatory landscape for upcoming health authority initiatives or projects, work directly with product management to translate regulatory requirements into Veeva’s framework, translate long and complex regulatory guidance into clear, concise information for different internal teams, and work with a team of Regulatory Intelligence Analysts to continually improve the processes and tools used for collecting, documenting, managing, and communicating regulatory intelligence.
Quality and regulatory software solutions provider
Veeva Systems offers software solutions for quality, regulatory, and advertising claims management, focusing on consumer products and chemical companies. Their cloud-based platform provides visibility and traceability throughout the product journey, ensuring compliance with regulations and accelerating time-to-market. Unlike competitors, Veeva has specialized expertise in both the Life Sciences and Chemical sectors, allowing them to effectively address industry-specific challenges. The company's goal is to help clients efficiently bring safe and compliant products to market.